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Hakonarson, Hakon

Children's Hospital of Philadelphia, Leonard Madlyn Abramson Research Center, Philadelphia, PA, USA

TitleYearPMID
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions. 2010 20154673
Functional impact of global rare copy number variation in autism spectrum disorders. 2010 20531469
Large copy-number variations are enriched in cases with moderate to extreme obesity. 2010 20622171
Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis. 2010 20053666
Rare variants create synthetic genome-wide associations. 2010 20126254
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. 2009 19404257
Common genetic variants on 5p14.1 associate with autism spectrum disorders. 2009 19404256
Genome-wide association analysis identifies PDE4D as an asthma-susceptibility gene. 2009 19426955
Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms. 2008 18784189
PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. 2007 17921354
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